RegWardenFDA facility compliance records
Facility

KARL STORZ VIDEO ENDOSCOPY ESTONIA OUE

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2016: 1 recalls; 2022: 1 inspections1201620172018201920202021120222023202420252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

  • Nasopharyngoscope (Flexible Or Rigid)
    Product code EOB (opens in a new tab) · Class II · Ear, Nose, Throat · 21 CFR 874.4760

Recalls & enforcement

  • Class IITerminated2016-02-29
    Endoscope cleaning brush 11276CL may not fit resulting in an inability to insert the brush in to the channel of the intended endoscope or to completely pass it through such channel.

FDA inspections (1)

  • NAI2022-11-17
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “KARL STORZ VIDEO ENDOSCOPY ESTONIA OUE (FEI 3004644065) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004644065-karl-storz-video-endoscopy-estonia-oue/

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